9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester

Base Information

• Chemical Name: 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester
• CAS No.: 112634-70-5
• Molecular Formula: C₂₂H₁₇ClFN₃O₃
• Molecular Weight: 425.847
• Mol file: 112634-70-5.mol

Synonyms:

Chemical Property of 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester

There total 5 articles about 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methoxy-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester (112634-66-9) + methylamine (74-89-5) → 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester (112634-70-5)

Guidance literature:

In ethanol; for 3h; Ambient temperature;

DOI:10.1002/jhet.5570240327

Reference yield:

7-chloro-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepine-2-acetic acid methyl ester (112634-51-2) → 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester (112634-70-5)

Guidance literature:

Multi-step reaction with 4 steps

1: 88 percent / benzene / 0.5 h / Heating

2: 1. sodium methoxide / 1. methanol, reflux, 5 min.; 2. dichloromethane, 30 min.

3: 64 percent / act. MnO₂ / toluene / 0.33 h / Heating

4: 80 percent / ethanol / 3 h / Ambient temperature

With manganese(IV) oxide; sodium methylate; In ethanol; toluene; benzene;

DOI:10.1002/jhet.5570240327

Reference yield:

9-chloro-7-(2-fluorophenyl)-1,4,4a,5-tetrahydro-3-methoxy-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester (112634-65-8) → 9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methylamino-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester (112634-70-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 64 percent / act. MnO₂ / toluene / 0.33 h / Heating

2: 80 percent / ethanol / 3 h / Ambient temperature

With manganese(IV) oxide; In ethanol; toluene;

DOI:10.1002/jhet.5570240327

upstream raw materials:

9-chloro-7-(2-fluorophenyl)-1,5-dihydro-3-methoxy-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester

methylamine

7-chloro-2,3-dihydro-5-(2-fluorophenyl)-1H-1,4-benzodiazepine-2-acetic acid methyl ester

9-chloro-7-(2-fluorophenyl)-1,4,4a,5-tetrahydro-3-methoxy-1-oxopyrido<1,2-a><1,4>benzodiazepine-2-carboxylic acid methyl ester